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. 2018 Sep 21;9(74):33961–33971. doi: 10.18632/oncotarget.26104

Table 3. Top 10 adverse events.

Cytotoxic Combination Trials (N=67) Molecularly Targeted Single Agent Trials (N=60)
Cycle 1 n (%) Cycles 2-6 n (%) Cycle 1 n (%) Cycles 2-6 n (%)
Diarrhoea 36 (53.7) Fatigue 24 (35.8) Fatigue 25 (41.7) Fatigue 20 (33.3)
Rasha 32 (47.8) Diarrhoea 19 (28.4) Diarrhoea 19 (31.7) Anorexia 12 (20.0)
Fatigue 28 (41.8) Mucositisb 18 (26.9) Nausea 18 (30.0) Diarrhoea 10 (16.7)
Mucositisb 23 (34.3) Alopecia 14 (20.9) Rasha 14 (23.3) Rasha 9 (15.0)
Nausea 22 (32.8) Rasha 12 (17.9) Mucositisb 9 (15.0) Vomiting 9 (15.0)
Pyrexia 16 (23.9) Vomiting 12 (17.9) Anorexia 8 (13.3) Nausea 9 (15.0)
Anorexia 11 (16.4) Nausea 10 (14.9) Dysgeusia 6 (10.0) Oedema 6 (10.0)
Constipation 9 (13.4) Anorexia 10 (14.9) Urine Discoloration 5 (8.3) Increased Bilirubin 5 (8.3)
Epistaxis 8 (11.9) Anaemia 9 (13.4) Dry Skin 5 (8.3) Mucositisb 5 (8.3)
Neutropeniac 8 (11.9) Neutropeniac 8 (11.9) Dyspepsia 5 (8.3) Pain 5 (8.3)

Ranked adverse events by trial type and cycle number, either cycle 1 or cycles 2-6. AEs were ranked to show top 10 in each trial and cycle group. AEs are displayed in ascending order of raw count with percentage incidence given in brackets.

a including pruritic, fungal, macropapular, acneiform, pustular.

b including stomatitis and coryzal symptoms.

c including resultant fever or sepsis.